Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1152591
rs1152591
1.000 0.080 14 64214130 intron variant A/C;G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.800 1.000 1 2012 2017
dbSNP: rs10459452
rs10459452
14 64245143 intron variant A/G snv 4.4E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs11850375
rs11850375
14 64244659 intron variant C/T snv 4.4E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs11850375
rs11850375
14 64244659 intron variant C/T snv 4.4E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12435857
rs12435857
0.925 0.200 14 64256807 intron variant G/A snv 0.41
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1256030
rs1256030
0.827 0.240 14 64280452 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1256031
rs1256031
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1256033
rs1256033
14 64278681 intron variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1256061
rs1256061
14 64236875 intron variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4365213
rs4365213
1.000 0.080 14 64253546 intron variant T/C snv 0.41
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012